Sitemap | Symptoma

16801 to 16900 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

Congenital Disorder of Glycosylation Type 2J Neoplasm of Ampulla of Vater Long QT Syndrome 13 Malignant Hepatic Neoplasm Neoplasm of Nasal Cavity Early Infantile Epileptic Encephalopathy Type 5 Intercostal Neuralgia 14q11-q22 Microdeletion Syndrome Microscopic Polyangiitis Dilated Cardiomyopathy 1R Homozygous Familial Hypercholesterolemia 15q24 Deletion Syndrome Early Infantile Epileptic Encephalopathy Type 10 Warsaw Breakage Syndrome Autosomal Recessive Deafness 84 Fanconi Anemia Complementation Group O Acute Amebic Dysentery Fanconi Renotubular Syndrome Type 2 Perforated Diverticulum Syndromic Multisystem Autoimmune Disease Brachydactyly Type E2 Distal Hereditary Motor Neuropathy Type 2C Maturity-Onset Diabetes of the Young Type 11 Maturity-Onset Diabetes of the Young Type 10 Viral Upper Respiratory Tract Infection Acute Subglottic Laryngitis Mild Mononeuropathy of the Median Nerve Nephronophthisis-Like Nephropathy Branch Retinal Vein Occlusion Muscular Dystrophy-Dystroglycanopathy Type C2 Migraine without Aura Muscular Dystrophy-Dystroglycanopathy Type C3 Muscular Dystrophy-Dystroglycanopathy Type B2 Muscular Dystrophy-Dystroglycanopathy Type B1 Muscular Dystrophy-Dystroglycanopathy Type A6 Muscular Dystrophy-Dystroglycanopathy Type A5 Muscular Dystrophy-Dystroglycanopathy Type B3 Muscular Dystrophy-Dystroglycanopathy Type A2 Common Variable Immunodeficiency Type 2 Congenital Disorder of Glycosylation Type 1Q Mantle Cell Lymphoma Bardet-Biedl Syndrome Type 15 Pilocytic Astrocytoma Keratosis Obturans Autosomal Dominant Polycystic Kidney Disease 1 Genetic Mosaic TK2-Related Myopathic Mitochondrial DNA Depletion Syndrome Passovoy Factor Defect Polyarticular Juvenile Idiopathic Arthritis Common Variable Immunodeficiency Type 1 Benign Familial Neonatal Epilepsy Type 1 Myelophthisis Limb-Girdle Muscular Dystrophy Type 1E Autosomal Recessive Deafness 76 Philadelphia Chromosome Positive Chronic Myeloid Leukemia Dentinogenesis Imperfecta Type 1 Recurrent Small-Cell Carcinoma of the Lung Meconium Ileus Opitz G/BBB Syndrome Type 1 Metastatic Ovarian Carcinoma Autosomal Dominant Spastic Paraplegia Type 37 Autosomal Dominant Spastic Paraplegia Type 36 Bardet-Biedl Syndrome Type 4 Bardet-Biedl Syndrome Type 2 Bardet-Biedl Syndrome Type 1 Spinocerebellar Ataxia Type 30 Generalized Myotonia of Thomsen Limb-Girdle Muscular Dystrophy Type 2D Fusarium Infection Pseudohypoparathyroidism Type 1C Condyloma Latum Focal Non-Epidermolytic Palmoplantar Keratoderma Quinine Poisoning Lymph Node Disorder Hereditary Factor X Deficiency Amelogenesis Imperfecta Type 1G with Nephrocalcinosis Adrenal Infarction Isolated Sulfite Oxidase Deficiency Hypogonadotropic Hypogonadism Myotonic Dystrophy Type 2 Zlotogora-Ogur Syndrome Neurofibromatosis-Noonan Syndrome Hereditary Prosopagnosia Growth Hormone Deficiency Infantile-Onset Ascending Hereditary Spastic Paralysis Immunodeficiency by Defective Expression of HLA Class 2 Autosomal Dominant Spastic Paraplegia Type 3 Autosomal Dominant Spastic Paraplegia Type 17 Leber Congenital Amaurosis Type 1 Infantile Onset Autophagic Vacuolar Myopathy Usher Syndrome Type 2C Nephropathic Cystinosis Athetoid Cerebral Palsy Crigler-Najjar Syndrome Type 2 Intracranial Mass Clark-Baraitser Syndrome Ruptured Ectopic Pregnancy Ectopic Pregnancy with Intrauterine Pregnancy Epidermolysis bullosa simplex with Muscular Dystrophy Retroverted Uterus